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Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida.

Journal articles  - Journal Article
Jasien, JM; Stout, JA; Mikati, MA; Anderson, RJ; Nave, BG; Fuchs, HE; Smith, B; Badea, A; Browndyke, JN
Published in: Ann Child Neurol Soc
September 2025

OBJECTIVE: Possible pleiotropic effects of apolipoprotein E4 (APOE E4) in individuals with congenital brain malformations are relatively unknown. Our goal was to determine if neurodegeneration-linked brain region volumes differ significantly between E4 carriers and noncarriers in young adults with spina bifida (SB). METHODS: Eleven individuals ( > 18 years), genotyped for APOE, underwent neuroimaging and neurocognitive evaluation. Primary analysis: Magnetic resonance imaging (MRI) data from 10 a priori neurodegeneration-risk regions of interest were compared between E4 carriers and noncarriers, adjusting for age, sex, and total intracranial volume (FDR-adjusted p < 0.05). Secondary analyses: Age-adjusted neurocognitive standard scores were compared between groups (p < 0.05). Post hoc analyses of NeuroQuant-derived regional brain volumes were examined for combined group differences in young adults with SB. RESULTS: Comparison of a priori risk region volumes revealed significantly lower left amygdala volumes (FDR-adjusted p = 0.04) in young adult E4 carriers (n = 4) relative to noncarriers (n = 7). Neurocognitive data were not significantly different between the groups. A possible trend was detected for enlarged parietal volumes in E4 carriers (p = 0.07), while volumetric extremes ( > 95% or < 5%) were detected for the anterior cingulate (100% of cases; p = 0.001), frontal cortices (90% of cases), hippocampus (80% of cases), and entorhinal cortices (70% of cases). INTERPRETATION: Early left amygdala volumetric reduction was found in E4 carriers; combined group volume comparisons revealed frontal and temporal lobe differences in young adults with SB relative to age- and sex-matched volumetric estimates. This pilot investigation does not appear to support E4 conferring a pleiotropic benefit in young adults with SB but rather supports further investigation of MRI volumetrics as a possible biomarker for this population.

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Published In

Ann Child Neurol Soc

DOI

EISSN

2831-3267

Publication Date

September 2025

Volume

3

Issue

3

Start / End Page

208 / 219

Location

United States
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Jasien, J. M., Stout, J. A., Mikati, M. A., Anderson, R. J., Nave, B. G., Fuchs, H. E., … Browndyke, J. N. (2025). Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida. Ann Child Neurol Soc, 3(3), 208–219. https://doi.org/10.1002/cns3.70016
Jasien, Joan M., Jacques A. Stout, Mohamad A. Mikati, Robert J. Anderson, Brittany G. Nave, Herbert E. Fuchs, Brian Smith, Alexandra Badea, and Jeffrey N. Browndyke. “Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida.Ann Child Neurol Soc 3, no. 3 (September 2025): 208–19. https://doi.org/10.1002/cns3.70016.
Jasien JM, Stout JA, Mikati MA, Anderson RJ, Nave BG, Fuchs HE, et al. Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida. Ann Child Neurol Soc. 2025 Sep;3(3):208–19.
Jasien, Joan M., et al. “Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida.Ann Child Neurol Soc, vol. 3, no. 3, Sept. 2025, pp. 208–19. Pubmed, doi:10.1002/cns3.70016.
Jasien JM, Stout JA, Mikati MA, Anderson RJ, Nave BG, Fuchs HE, Smith B, Badea A, Browndyke JN. Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida. Ann Child Neurol Soc. 2025 Sep;3(3):208–219.

Published In

Ann Child Neurol Soc

DOI

EISSN

2831-3267

Publication Date

September 2025

Volume

3

Issue

3

Start / End Page

208 / 219

Location

United States